S. M. Jaleel & Company Limited

3 records, newest first. Each line links to the FDA page it came from.

Refusal charges, in plain English

• NUTRIT LBL1 refused line

  Nutrition information missing from label

  The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.

• UNSAFE COL1 refused line

  Color additive unsafe under section 721

  The product appeared to be, or to contain, a color additive that is unsafe within the meaning of section 721(a) of the FD&C Act, the section that governs which color additives may be used and how.

Questions about S. M. Jaleel & Company Limited

Is S. M. Jaleel & Company Limited on an FDA import alert?

Yes. As of October 26, 2026, S. M. Jaleel & Company Limited is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for carbonated soft drink/ chubby reggae red-hibiscus flavor; FDA published the listing on April 13, 2015.

Has FDA refused shipments from S. M. Jaleel & Company Limited?

Yes. FDA refused 1 shipment line from S. M. Jaleel & Company Limited on July 10, 2026. The most recent, on July 10, 2026, was beer (nonalcoholic beverages), charged as UNSAFE COL (color additive unsafe under section 721).

Why did FDA refuse S. M. Jaleel & Company Limited's shipments?

The most frequent charges are NUTRIT LBL (nutrition information missing from label, 1 line) and UNSAFE COL (color additive unsafe under section 721, 1 line).

When was S. M. Jaleel & Company Limited last inspected by FDA?

FDA's most recent inspection of S. M. Jaleel & Company Limited with a final classification is dated May 24, 2017 and was classified NAI (No Action Indicated).

What is S. M. Jaleel & Company Limited's FEI number?

S. M. Jaleel & Company Limited's FDA Establishment Identifier (FEI) is 1000233425.

Can shipments from S. M. Jaleel & Company Limited still enter the U.S.?

Shipments of carbonated soft drink/ chubby reggae red-hibiscus flavor from S. M. Jaleel & Company Limited can be detained without physical examination under Import Alert 45-02; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).